Gv. Doone et al., Distribution of NADPH-d and nNOS-IR in the thoracolumbar and sacrococcygeal spinal cord of the guinea pig, J AUTON NER, 77(2-3), 1999, pp. 98-113
The distribution of NADPH-d staining and neuronal nitric oxide synthase (nN
OS)-immunoreactivity in the spinal cord of the guinea pig was studied to ev
aluate the potential role of nitric oxide in lumbosacral afferent and spina
l autonomic pathways and to compare the distribution of these two markers t
o that observed in other species. NADPH-d staining and nNOS-immunoreactivit
y were present in neurons and fibers in the superficial dorsal hem, dorsal
commissure and in neurons around the central canal in all levels of the spi
nal cord examined. Sympathetic preganglionic neurons in the thoracic and ro
stral lumbar segments identified by choline acetyl transferase (ChAT) immun
oreactivity exhibited prominent NADPH-II staining and nNOS-immunoreactivity
; whereas the ChAT-immunoreactive parasympathetic preganglionic neurons in
the sacral segments were not stained. The most prominent NADPH-d staining i
n the sacral segments occurred in fibers extending from Lissauer's tract th
rough laminae I along the lateral edge of the dorsal horn to the region of
the sacral parasympathetic nucleus (lateral collateral pathway of Lissauer)
. These fibers were prominent in the S1-S3 segments but not in adjacent (L5
-L7 and Cx1) or thoracolumbar segments. These NADPH-d fibers were, for the
most part, not nNOS-immunoreactive, but did overlap with a prominent fiber
bundle containing vasoactive intestinal polypeptide immunoreactivity in the
sacral spinal cord. These results indicate that nitric oxide may function
as a transmitter in thoracolumbar sympathetic preganglionic neurons, but no
t in sacral parasympathetic preganglionic neurons. Although the functional
significance of the NADPH-d positive, nNOS-negative fiber bundle on the lat
eral edge of the sacral dorsal horn remains to be determined, this fiber tr
act may represent, in part, visceral afferent projections to the sacral par
asympathetic nucleus. (C) 1999 Elsevier Science B.V. All rights reserved.